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239 Cards in this Set
- Front
- Back
Acebutolol
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β1 partial agonist
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Acetylcholine
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Endogenous AChR agonist
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Adrenaline
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Endogenous α2/β2 agonist
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Aspirin
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NSAID, Irreversible COX1-3 inhibitor
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Atropine
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mAChR antagonist, Competitive
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Benzilylcholine mustard
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AChR antagonist Irreversible
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α-bungarotoxin
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NMJ nAChR antagonist, Irreversible
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Buprenorphine
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μ partial agonist, Orally active
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Cimetidine
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H2 antagonist, Peptic ulcer treatment
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Cyanopindolol
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β1 antagonist, Commonly 125I radiolabelled
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Fexofenadine
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H1 antagonist, Does not penetrate BBB
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Imatinib
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Bcr-Abl inhibitor, Treatment of CML
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Heroin
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μ agonist, Acetylated form of morhpine, crosses BBB more readily
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Isoprenaline
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β agonist
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Mecamylamine
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Neuronal nAChR antagonist
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Misoprostol
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EP3 agonist, Synthetic prostaglandin EP1 analogue, peptic ulcer treatment
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Morphine
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μ agonist
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Naloxone
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μ antagonist, Treatment of opioid overdose
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Nicotine
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nAChR agonist
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Noradrenaline
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Endogenous α1/β1 agonist
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Omeprazole
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Gastic parietal cell proton pump inhibitor, Peptic ulcer treatment
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Paracetamol
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NSAID, COX1-3 inhibitor
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Pilocarpine
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mAChR agonist
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Prazosin
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α1 antagonist
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Propanolol
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β antagonist
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Pyrilamine
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H1 antagonist, Penetrates BBB
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Terfenadine
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H1 antagonist, Prodrug, does not penetrate BBB
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Yohimbine
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α2 antagonist
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Metformin
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Mimics insulin effects
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Sulphonylureas
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K+ATP channel inhibitor, Promotes insulin release by depolarising β cells, allowing Ca2+ influx which causes exocytosis
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Meglitinide
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K+ATP channel inhibitor, Promotes insulin release by depolarising β cells, allowing Ca2+ influx which causes exocytosis (lower affinity than sulphonylureas)
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Thiazolidinedione
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PPAR agonist, Activates TFs which promote FA storage and glucose metabolism
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Acarbose
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α-glucosidase inhibitor, Reduces glucose intake from GIT
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BoNT-A
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Neurotoxin, Cleaves SNAP-25
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BoNT-B
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Neurotoxin, Cleaves synaptobrevin
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BoNT-C
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Neurotoxin, Cleaves SNAP-25 and syntaxin
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BoNT-D
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Neurotoxin, Cleaves synpatobrevin
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BoNT-E
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Neurotoxin, Cleaves SNAP-25
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BoNT-F
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Neurotoxin, Cleaves synaptobrevin
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BoNT-G
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Neurotoxin, Cleaves synaptobrevin
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TeNT
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Neurotoxin, Cleaves synaptobrevin
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Hemicholium
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ChT inhibitor
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Triethylcholine
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CAT competitive substrate
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Vesamicol
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VAChT inhibitor
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β-bungarogtoxin
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PLA2 activity, In cholinergic nerves
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Taipoxin
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PLA2 activity, In cholinergic nerves
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α-latrotoxin
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Forms Ca2+ permeable channels, In cholinergic nerves
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Trimetaphan
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Ganglionic nAChR antagonist, Competitive
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Hexamethonium
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Ganglionic nAChR antagonist
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Decamethonium
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NMJ nAChR antagonist
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d-tubocurarine
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nAChR antagonist
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Pancuronium
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Non-depolarising NMJ blocker
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Rocuronium
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Non-depolarising NMJ blocker
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Atracurium
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Non-depolarising NMJ blocker
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Mivacurium
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Non-depolarising NMJ blocker
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Sugammadex
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Non-depolaring blockade reversal, Binds steroidal non-depolarising blockers
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Suxamethonium
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Depolarising NMJ blocker
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Carbachol
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AChR agonist
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Methacholine
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mAChR agonist
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Cevimeline
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M3 agonist
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Tropicamide
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mAChR antagonist, Short acting
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Ipratopium
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mAChR antagonist
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Pirenzepine
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M1 antagonist
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Darifenicin
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M3 antagonist
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Edrophonium
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AChE Inhibitor, Short acting
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Tacrine
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AChE Inhibitor, Short acting
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Donezepil
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AChE Inhibitor, Short acting
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Neostigmine
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AChE Inhibitor, Medium acting
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Pyridostigmine
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AChE Inhibitor, Medium acting
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Rivastigmine
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AChE Inhibitor, Medium acting
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Dyflos
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AChE Inhibitor, Long acting
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Ecothiapate
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AChE Inhibitor, Long acting
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Malathion
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AChE Inhibitor, Long acting
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Pralidoxime
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AChE reactivator
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a-methyltyrosine
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Tyrosine hydroxylase inhibitor, Competitive
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L-DOPA
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DOPA decarboxylase substrate
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Carbidopa
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DOPA decarboxylase inhibitor
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Benserazide
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DOPA decarboxylase inhibitor
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Droxidopa
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NA precursor
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Disulfiram
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Dopamine β hydroxylase inhibitor
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Methyldopa
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False transmitter precursor
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6-hydroxydopamine
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Neurotoxin, Kills noradrenergic nerves
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Reserpine
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VMAT inhibitor
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Ephedrine
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Sympathomimetic monoamine, Indirect
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Dextroamphetamine
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Sympathomimetic monoamine, Indirect
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Guanethidine
|
NA release inibitor
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Desiprimine
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NET inhibitor
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Amitriptyline
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NET/SERT inhibitor
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Fluoxetine
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SSRI
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Citalopram
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SSRI
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Cocaine
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NET/SERT/DAT inhibitor
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Phenoxybenzamine
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Irreversible α1/α2 antagonist
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Moclobemide
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MAO-A inhibitor
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Selegiline
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MAO-B inhibitor
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Entacapone
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COMT inhibitor
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Phenylephrine
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α1/α2 agonist
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Methoxamine
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α1/α2 agonist
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Clonidine
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α2 agonist, Relatively selective, also activates I receptors
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Xylazine
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α2 agonist, Relatively selective
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Dexmedetomidine
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α2 agonist, Relatively selective
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Dobutamine
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β1 agonist
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Salbutamol
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β2 agonist, Short acting
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Salmeterol
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β2 agonist, Long acting
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Formoterol
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β2 agonist, Long acting
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Indacaterol
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β2 agonist, Ultra long lasting
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Mirabegron
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β3 agonist
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Labetalol
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α/β antagonist
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Phentolamine
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α1/α2 antagonist
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Doxazosin
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α1 antagonist
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Tamsulosin
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α1A antagonist
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Propranolol
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β1/β2 antagonist
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Atenolol
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β1 antagonist
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Nebivolol
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β1 antagonist, Metabolite is β3 agonist
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Caffeine
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A1 antagonist
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Dipyramidole
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NsT inhibitor
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Desmopressin
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ADH synthetic analogue
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Glyceryl trinitrate
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NO donor
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Sildenafil
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PDE V inhibitor
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Alprostadil
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PGE1 analogue
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Amyl nitrite
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NO donor
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L-NAME
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NOS inhibitor, Non-selective
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7-NI
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Neuronal NOS inhibitor
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L-NIO
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iNOS inhibitor, Irreversible
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Bacitracin
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Peptidoglycan synthesis inhibitor, Inhibits dephosphorylation of bactoprenol pyrophosphate carrier
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D-cycloserine
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Peptidoglycan synthesis inhibitor, D-Ala analogue, L-Ala racemase/D-Ala-D-Ala synthetase/D-Ala-D-Ala muramyl tripeptide ligase inhibitor
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Fosfomycin
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Peptidoglycan synthesis inhibitor, Pyruvyl transferase inhibitor
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Isoniazid
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Mycolic acid synthesis inhibitor, First line TB treatment
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Penicillin
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Peptidoglycan synthesis inhibitor, β-lactam antibiotic
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Ampicillin
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Peptidoglycan synthesis inhibitor, β-lactam antibiotic
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Amoxicillin
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Peptidoglycan synthesis inhibitor, β-lactam antibiotic
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Methicillin
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Peptidoglycan synthesis inhibitor, β-lactam antibiotic
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Clavulanate
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β-lactamase inhibitor
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Augmentin
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Amoxicillin/Clavulanate combination therapy
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Vancomycin
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Peptidoglycan synthesis inhibitor, Prevents D-Ala-D-Ala cross-linking
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Chloramphenicol
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Protein synthesis inhibitor, Prevents aminoacyl tRNA binding to 50s subunit
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Erythromycin
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Protein synthesis inhibitor, Macrolide, blocks polypeptide exit tunnel
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Fusidic acid
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Protein synthesis inhibitor, Binds EF-G, preventing movement of 30s subunit
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Streptomycin
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Protein synthesis inhibitor, Aminoglycoside, targets 30s subunit and decreases translation fidelity
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Gentamycin
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Protein synthesis inhibitor, Aminoglycoside, targets 30s subunit and decreases translation fidelity
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Tetracycline
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Protein synthesis inhibitor, Binds 30s subunit and inhibits movement of aminoacyl tRNA into A site
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Bleomycin
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Nucleic acid antibiotic, Metal-chelating, generates ROS to cause single and double strand breaks
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Ciprofloxacin
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DNA gyrase inhibitor, Fluoroquinolone, cause DNA supercoiling
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Daunomycin
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Cytotoxic drug, Intercalates dsDNA and causes local unwinding
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Mitomycin C
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Nucleic acid antibiotic, Alkylates and cross-links DNA
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Rifampin
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RNA polymerase inhibitor
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Sulfamethoxazole
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Antimetabolite antibiotic, Competitively inhibits dihydropterate synthase in tetrahydrofolate synthesis
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Trimethoprim
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Antimetabolite antibiotic, Inhibits dihydrofolate reductase in tetrahydrofolate synthesis
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Co-trimoxazole
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Sulfamethoxazole/Trimethoprim combination therapy
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Amphotericin B
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Membrane antibiotic, Targets ergosterol in fungal and parasitic membranes, pore-forming
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Flucanazole
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Membrane antibiotic, Inhibits ergosterol synthesis
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Miconazole
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Membrane antibiotic, Inhibits ergosterol synthesis
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Gramicidin A
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Membrane antibiotic, Ion channel forming
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Polymixin
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Membrane antibiotic, Cationic detergent, alters membrane permeability
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Valinomycin
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Membrane antibiotic, K+ transmembrane shuttle
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Artemisinin
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Antiparasitic, Produces ROS in RBC stage
|
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Chloroquine
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Antiparasitic, Inhibits haem polymerisation, toxic to plasmodium
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Mefloquine
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Antiparasitic, Inhibits haem polymerisation, toxic to plasmodium
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Clorsulon
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Antiparasitic, Phosphoglycerate kinase/mutase inhibitor
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Closantel
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Antiparasitic, Oxidative phosphorylation uncoupler
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Diclorvos
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Antiparasitic, Cholinesterase inhibitor, spastic paralysis
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Ivermectin
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Antiparasitic, Opens chloride channels, hyperpolarisation
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Levamisole
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Antiparasitic, Nicotinic agonist, spastic paralysis
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Melarsen
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Antiparasitic, Arsenic compound, selectively accumulated
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Paraherquamide
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Antiparasitic, Nicotinic antagonist, flaccid paralysis
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Praziquantel
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Antiparasitic, Increase Ca2+ permeability
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Pyrimethamine
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Antiparasitic, Dihydrofolate reductase inhibitor (trimethoprim analogue)
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Sulfadoxin
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Antiparasitic, Dihydropterate synthase inhibitor (sulfamethoxazole analogue)
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Suramin
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Antiparasitic (mechanism unknown), P2X antagonist
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Thiobenzdole
|
Antiparasitic, Enhances tubulin depolymerisation
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Acyclovir
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Antiviral, Activated by viral thymidine kinase, inhibits viral DNA polymerase
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Amantadine
|
Antiviral, M2 channel antagonist, prevents influenza acidification
|
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Gancyclovir
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Antiviral, Activated by viral thymidine kinase, inhibits viral DNA polymerase
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Cidofovir
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Antiviral, Cytosine analogue, inhibits viral DNA polymerase
|
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Foscarnet
|
Antiviral, Pyrophosphate analogue, inhibits viral DNA polymerase
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Interferon
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Antiviral, Immunoregulatory cytokine
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Nevirapine
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Antiviral, HIV non-nucleoside RT inhibitor
|
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Oseltamivir
|
Antiviral, Neuraminidase inhibitor
|
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Zanamivir
|
Antiviral, Neuraminidase inhibitor
|
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Saquinavir
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Antiviral, HIV protease inhibitor
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Zidovudine
|
Antiviral, Thymidine analogue, RT inhibitor
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AZT
|
Antiviral, Thymidine analogue, RT inhibitor
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HAART
|
Nevirapine/Zidovudine/Saquinavir combination therapy
|
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5-Fluorouracil
|
Anticancer, Antimetabolite, thymidylate synthase inhibitor
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Cyclophosphamide
|
Anticancer, Alkylating agent
|
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Lomustine
|
Anticancer, Alkylating agent, lipid soluble
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Carmustine
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Anticancer, Alkylating agent, lipid soluble
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Dactinomycin
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Anticancer, Intercalating agent
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Doxorubicin
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Anticancer, Causes oxidative DNA damage
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Taxol
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Anticancer, Stabilises mitotic spindle
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Colchicine
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Anticancer, Prevents tubulin assembly
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Tamoxifen
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Anticancer, ERα antagonist
|
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Herceptin
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Anticancer, Her2 antagonist
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Ipilimumab
|
Anticancer, Targets CTLA-4
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Parp inhibitors
|
Anticancer, Synthetic lethality
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Lidocaine
|
Local anaesthetic, Class IB antidysrhythmic, vNa antagonist
|
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Lamotrigine
|
Local anaesthetic, vNa antagonist
|
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Tetrodotoxin
|
Neurotoxin, vNa antagonist
|
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Phenytoin
|
Anticonvulsant, vNa antagonist
|
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Kainate
|
AMPA agonist
|
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Alteplase
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Plasminogen activator
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Desmoteplase
|
Plasminogen activator
|
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Topiramate
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Anticonvulsant
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Valproate
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Anticonvulsant
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Batrachotoxin
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vNa agonist, Prevents inactivation
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α-scorpion toxin
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vNa agonist, Prevents inactivation
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Verapamil
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Phenylalkylamine, class IV antidysrhythmic, L-type Ca2+ channel antagonist
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Nifedipine
|
Dihydropyridine, L-type Ca2+ channel antagonist
|
|
BAY K 8664
|
Dihydropyridine, L-type Ca2+ channel agonist
|
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Diltiazem
|
Benzothiazepine, L-type Ca2+ channel antagonist
|
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Quinidine
|
Class IA antidysrhythmic
|
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Flecainide
|
Class IC antidysrhythmic
|
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Amiodarone
|
Class III antidysrhythmic, Mechanism unknown, prolongs AP
|
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Digoxin
|
Na+/K+-ATPase inhibitor, Cardiac glycoside
|
|
Digitoxin
|
Na+/K+-ATPase inhibitor, Cardiac glycoside
|
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Oubain
|
Na+/K+-ATPase inhibitor, Cardiac glycoside
|
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Theophylline
|
PDE inhibitor
|
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Milrinone
|
PDE inhibitor
|
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Mannitol
|
Osmotic diuretic, Increases tubular osmotic pressure
|
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Acetazolamide
|
Carbonic anhydrase inhibitor
|
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Furosemide
|
Loop diuretic, Inhibits NKCC
|
|
Bendroflumethiazide
|
Thiazide diuretic, Inhibits Na+/Cl- antiporter
|
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Hydrochlorothiazide
|
Thiazide diuretic, Inhibits Na+/Cl- antiporter
|
|
Spironolactone
|
AT1R antagonist
|
|
Amiloride
|
ENAC blocker
|
|
Glycyrrhetinic acid
|
11β-HSD inhibitor
|
|
Catopril
|
ACE inhibitor
|
|
Enalapril
|
ACE inhibitor
|
|
Losartan
|
AT1R antagonist
|
|
Valsartan
|
AT1R antagonist
|
|
Simvastatin
|
HMG-CoA reductase inhibitor, Reversible
|
|
Lovastatin
|
HMG-CoA reductase inhibitor, Reversible
|
|
Atorvastatin
|
HMG-CoA reductase inhibitor, Long acting
|
|
Bezafibrate
|
PPARα agonist, Reduce VLDL and LDL levels
|
|
Ciprofibrate
|
PPARα agonist, Reduce VLDL and LDL levels
|
|
Clofibrate
|
PPARα agonist, Reduce VLDL and LDL levels
|
|
Ezaetimibe
|
NPC1L1 blocker, Reduces cholesterol absorption
|
|
Isosorbide mononitrate
|
NO donor
|
|
Ivabradine
|
HCN blocker, Inhibits If at SAN
|
|
Ranolazine
|
vNa antagonist, Reduces late Na+ current in cardiac AP
|